ClinGen Allele Registry
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Canonical Allele Identifier:
PA915977323
Gene: MAPT
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000015324
RCV000084553
RCV000517183
RCV001851871
ClinVar Variation:
14255
98232
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001116538.2:p.Gly724Arg
CA225494
NM_001123066.4:c.2170G>C
CA257189
NM_001123066.4:c.2170G>A